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关于此项目
经验公式（希尔记法）:
C30H59NO2
化学文摘社编号:
分子量:
465.79
MDL number:
NACRES:
NA.25
UNSPSC Code:
12352211
产品名称
N-C12-deoxysphingosine, N-lauroyl-1-deoxysphingosine (m18:1/12:0), powder
assay
>99% (TLC)
form
powder
packaging
pkg of 1 × 1 mg (860455P-1mg), pkg of 1 × 5 mg (860455P-5mg)
manufacturer/tradename
Avanti Research™ - A Croda Brand 860455P
lipid type
sphingolipids
bioactive lipids
shipped in
dry ice
storage temp.
−20°C
General description
N-C12-deoxysphingosine, also known as 1-deoxydihydroceramide (1-deoxyDHCer) is, the N-acylated form of 1-deoxysphinganine, a potent inhibitor of sphingolipid metabolism.
Application
N-C12-deoxysphingosine has been used as a standard in the quantitation of atypical sphingoid bases in biological samples by reverse-phase liquid chromatography coupled to electrospray ionization tandem mass spectrometry (LC-MS/MS).
Packaging
5 mL Amber Glass Screw Cap Vial (860455P-1mg)
5 mL Amber Glass Screw Cap Vial (860455P-5mg)
Legal Information
Avanti Research is a trademark of Avanti Polar Lipids, LLC
存储类别
11 - Combustible Solids
wgk
WGK 3
Junliang Wan et al.
Journal of agricultural and food chemistry, 67(46), 12953-12961 (2019-10-23)
Most common sphingolipids are comprised of "typical" sphingoid bases (sphinganine, sphingosine, and structurally related compounds) and are produced via the condensation of l-serine with a fatty acyl-CoA by serine palmitoyltransferase. Some organisms, including mammals, also produce "atypical" sphingoid bases that
Sarah T Pruett et al.
Journal of lipid research, 49(8), 1621-1639 (2008-05-24)
"Sphingosin" was first described by J. L. W. Thudichum in 1884 and structurally characterized as 2S,3R,4E-2-aminooctadec-4-ene-1,3-diol in 1947 by Herb Carter, who also proposed the designation of "lipides derived from sphingosine as sphingolipides." This category of amino alcohols is now
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 860455P-1MG | 04061835316953 |
| 860455P-5MG | 04061835316960 |